FDA Inspection 1193488 — Medifactia AB

Medifactia AB — FEI 3015871081

The FDA completed an inspection of Medifactia AB on November 14, 2022 in Stockholm. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
November 14, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Stockholm (Sweden)